Marine turtles are only minimally sexually size dimorphic,a pattern that is distinct from most nonmarine aquatic turtles

Turtles have been prominent subjects of sexual size dimorphism (SSD) analyses due to their compact taxonomy, mating systems, and habitat diversity. In prior studies, marine turtles were grouped with fully aquatic non‐marine turtles (NMATs). This is interesting because it is well‐established that the marine environment imposes a distinct selective milieu on body form of vagile vertebrates, driven by convergent adaptations for energy‐efficient propulsion and drag reduction. We generated a comprehensive database of adult marine turtle body sizes (38,569 observations across all species), which we then used to evaluate the magnitude of SSD in marine turtles and how it compares to SSD in NMAT. We find that marine turtles are only minimally sexually size dimorphic, whereas NMAT typically exhibit female‐biased SSD. We argue that the reason for this difference is the sustained long‐distance swimming that characterizes marine turtle ecology, which entails significant energetic costs incurred by both sexes. Hence, the ability of either sex to allocate proportionately more to growth than the other is likely constrained, meaning that sexual differences in growth and resultant body size are not possible. Consequently, grouping marine turtles with NMAT dilutes the statistical signature of different kinds of selection on SSD and should be avoided in future studies.     

Reproductive Biology of Captive Green Sea Turtles Chelonia mydas

A captive colony of green sea turtles, Chelonia mydas, has beenmaintained and observed at a commercial sea turtle farm on GrandCayman Island, B.W.I., since 1973. Observations of this breedingcolony show that the mating and nesting behaviour of the captivegreen sea turtle is similar to that observed in wild populations.Evidence indicates that mating observed prior to a female'snesting in a given season determines the hatchabilityof thatseason's egg production. Annual per female egg production ofthe captive colony appears to be two to five times greater thanthat reported for wild colonies. Observations on the reproductivebiology of green sea turtles hatched and raised under farm conditionssuggests that the minimum age of sexual maturity is eight tonine years of age. The number of eggs per nest, the number ofnests per season per female and hatch rate tend to increasewith successive seasons nesting for these turtles reaching sexualmaturity.     

Spectral Sensitivities and Color Signals in a Polymorphic Damselfly

Animal communication relies on conspicuous signals and compatible signal perception abilities. Good signal perception abilities are particularly important for polymorphic animals where mate choice can be a challenge. Behavioral studies suggest that polymorphic damselflies use their varying body colorations and/or color patterns as communication signal for mate choice and to control mating frequencies. However, solid evidence for this hypothesis combining physiological with spectral and behavioral data is scarce. We investigated this question in the Australian common blue tail damselfly, Ischnura heterosticta, which has pronounced female-limited polymorphism: andromorphs have a male-like blue coloration and gynomorphs display green/grey colors. We measured body color reflectance and investigated the visual capacities of each morph, showing that I. heterosticta have at least three types of photoreceptors sensitive to UV, blue, and green wavelength, and that this visual perception ability enables them to detect the spectral properties of the color signals emitted from the various color morphs in both males and females. We further demonstrate that different color morphs can be discriminated against each other and the vegetation based on color contrast. Finally, these findings were supported by field observations of natural mating pairs showing that mating partners are indeed chosen based on their body coloration. Our study provides the first comprehensive evidence for the function of body coloration on mate choice in polymorphic damselflies.     

Melanin‐Based Coloration Covaries with Hiding and Exploratory Behavior in Male Spanish Terrapins

Melanin‐based coloration reflects mostly social status and dominance in males of several species. However, the relation of melanism with other suites of behavioral traits has received less attention. Here, we examined whether the melanic coloration of the shell of male Spanish terrapins Mauremys leprosa was related to several behavioral patterns. To test this, we simulated predatory attacks of different risk levels and measured the time that the turtles spent hiding entirely in their own shells (i.e. appearance times). We also measured the activity level of the turtles in a novel‐environment test. The results showed that melanin‐based coloration was related to antipredatory behavior. Male terrapins with a greater extent of black coloration in their shells demonstrated shorter appearance times after a predator attack. However, this pattern was significant only when turtles were subjected to a high risk. In addition, darker turtles had longer latency times in a novel environment. The results of the present study support the hypothesis that melanin‐based coloration may be associated with some behavioral functions. Our study provides a good framework for future studies concerning the effect of melanin‐coloration on multiple behavioral traits that could be applied to further research using other animal models.     

Phylogenetic Patterns of Sexual Size Dimorphism in Turtles and Their Implications for Rensch’s Rule

Sexual size dimorphism (SSD) is widespread in nature and may result from selection operating differentially on males and females. Rensch’s rule, the increase of SSD with body size in male-biased-SSD species (or decrease in female-biased-SSD species), is documented in invertebrates and vertebrates. In turtles, evidence for Rensch’s rule is inconclusive and thus the forces underlying body size evolution remain obscure. Using a phylogenetic approach on 138 turtle species from 9 families, we found that turtles overall and three families follow Rensch’s rule, five families display isometry of SSD with body size, while Podocnemididae potentially follows a pattern opposite to Rensch’s rule. Furthermore, male size evolves at faster rates than female size. Female-biased-SSD appears ancestral in turtles while male-biased-SSD evolved in every polytypic family at least once. Body size follows an Ornstein–Uhlenbeck evolutionary model in both sexes and SSD types, ruling out drift as a driving process. We explored whether habitat type or sex determination might be general drivers of turtle body size evolution using a phylogenetic context. We found that males are proportionally larger in terrestrial habitats and smaller in more aquatic habitats, while the sex-determining mechanism had no influence on body size evolution. Together, our data indicate that Rensch’s rule is not ubiquitous across vertebrates, but rather is prevalent in some lineages and not driven by a single force. Instead, our findings are consistent with the hypotheses that fecundity-selection might operate on females and ecological-selection on males; and that SSD and sex-determining mechanism evolve independently in these long-lived vertebrates.     

Inter‐individual Variation in Antipredator Hiding Behavior of Spanish Terrapins Depends on Sex,Size, and Coloration

Behavioral responses to predation risk are critical for survival but as antipredator behavior is costly, prey animals should flexibly modulate their optimum defensive responses by considering both costs and benefits, which are partly influenced by the individual characteristics of the prey. Turtles have the shell as a morphological structure that may provide partial protection against predators, but hiding into the shell may entail some high costs, and turtles should decide when to switch to an active escape strategy to safe refuges. Here, we examined how gender, body size, and sexual coloration influence inter‐individual variability of antipredatory hiding behavior into the shell of Spanish terrapins (Mauremys leprosa). We simulated predatory attacks under different conditions and measured the time that the turtles spent hidden entirely inside the shell (i.e., appearance times) and from then until the turtle started to flee actively (i.e., waiting times). Our results showed that when risk increased, appearance times increased but waiting times decreased. When turtles were in a prone position, their hiding behavior was related with their body weight with heavier turtles having longer appearance times. Also, the conspicuousness of limb coloration was important for the appearance times of males, but not for females. Thus, males with brighter coloration of the limb stripes had longer appearance times than duller ones. In addition, when turtles were overturned, males appeared out of the shell earlier than females and heavier turtles started to right sooner, but only when risk was low. However, when turtles were overturned and risk was high, they should assume that they have already been detected, making inter‐individual differences in size and coloration apparently unimportant for deciding hiding behavior.     

Identifying Hot Moments in Road-Mortality Risk for Freshwater Turtles

ABSTRACT Risk assessments can be used to identify threats, which vary both in space and time, to declining species. Just as hot spots describe locations where threat processes operate at a higher rate than in surrounding areas, hot moments refer to periods when threat rates are highest. However, the identification of hot moments can be challenging because the temporal complexity of some threat processes makes their effects on population viability difficult to predict. Declining throughout much of their range, Blanding's turtle (Emydoidea blandingii) populations are potentially most vulnerable to road mortality where road densities and traffic volumes are high. The temporal variations in road-mortality risk faced by these and other semiaquatic turtles at the population level are a consequence of several factors, including sex-specific movement characteristics and seasonal changes in traffic volume. We examined these risk factors for Blanding's turtle populations in Maine, USA, by integrating temporally explicit roadkill probabilities with demographic parameters informed by local and range-wide studies. Specifically, we used population simulations to estimate the relative risk for 14 2-week periods during the turtles’ active season. Our analysis clearly identified early summer as a period of elevated risk, with June through mid-July signaling a road-mortality hot moment for Blanding's turtles (for both M and F). These findings provide guidance for the implementation of temporally explicit conservation measures such as cautionary road signage, traffic management, and public outreach that, if timed strategically, could help to mitigate population impacts from road mortality.     

Turtles as diapsid reptiles

Recent molecular studies of amniote relationships show turtles to be diapsid reptiles, related to the archosauromorph branch of saurian phylogeny. This conflicts with palaeontological data which shows turtles to be related either to anapsids, or to the lepidosauromorph branch within diapsids. Archosauromorph relationships of turtles have previously been proposed on the basis of neontological (mostly soft anatomy) characters. This paper reviews the neontological character evidence for turtle relationships and shows that most, but not all, of these characters are invalid in the reconstruction of turtle relationships within Amniota.     

First report of rapid eye color change in a non-avian tetrapod

Like coloration of the integument, eye color can be a significant but understudied component of communication and reproductive behavior. Eye color can change with sexual maturation and become sexually dimorphic, but in a few birds and fish, eye color can also change rapidly in response to the environment. There are few cases of the latter, and we report here several instances of such change in eye color in the Eastern box turtle (Terrapene carolina carolina), the first non-avian tetrapod in which this capability has been reported. In male turtles, the iris changed from a pale yellow color (often characteristic of juveniles) to a bright red color (characteristic of mature males) in a period of <5 s. The nature of the color change is similar to that observed in some birds and suggests a common mechanism and/or adaptive role, which could be further explored in Eastern box turtles.     

H-Y Antigen and Sex-Determination in Turtles

H-Y antigen was investigated in 14 turtle species belonging to five different families. In 13 species the female was typed as H-Y antigen positive, only in Chinemys reevesi was the male H-Y antigen positive. Since in all vertebrate species studied till now, the expression of H-Y antigen is strictly correlated with the heterogametic sex, it can be assumed that in turtles both types of sex determining mechanisms are realized, namely the ZZ/ZW-and the XX/XY mechanism; both mechanisms are realized in species belonging to one and the same turtle family. However, most turtle species seem to be endowed with a ZZ/ZW sex determining mechanism.     

Loss of sexual dimorphism is associated with loss of lekking behavior in the green manakin Xenopipo holochora

Manakins (Pipridae) are well know for elaborate male sexual displays and ornate plumage coloration, both of which are thought to have evolved as a consequence of lekking breeding, the prevalent mating system in the family. Less attention has been paid to a handful of ‘drab’ manakin species, in which sexual dimorphism appears to be reduced or absent. Using character reconstruction, we show that these ‘exceptions to the rule’ represent phylogenetically independent cases of losses in sexual dimorphism, and as such could provide a focal group to investigate the link between changes in morphology and in life history (e.g. mating system). We take a first step in this direction by focusing on two subspecies of the putatively monomorphic green manakin Xenopipo holochlora to formally confirm that the species is sexually monomorphic in size and plumage color and test the prediction that sexual monomorphism is associated with the loss of lekking behavior in this species. Our results show that size dimorphism is present but limited in the green manakin, with substantial overlap in male and female morphometric measures, and that sexes are largely monochromatic (including from an avian perspective), despite marked coloration differences between subspecies. Behavioral observations indicate that males do not form leks and do not engage in elaborate sexual displays, that there is no stable pair bond formation, and that females provide parental care alone. These findings are consistent with the idea that changes in mating behavior may have driven changes in morphology in Pipridae, and we encourage similar studies on other drab manakins to better understand this relationship.     

Precocious Courtship and Play in Emydid Turtles

In many mammal species, precocious sexual behaviour is a component of play. A recent model for the evolution of play fighting behaviour in muroid rodents by Pellis (1993) proposes that social play in those species has its origin in precocious sexual behaviour. Captive juvenile emydid turtles perform precocious sexual behaviour. After reviewing its occurrence, we focus on detailed observations of Pseudemys nelsoni. Precocious sexual behaviour in these turtles is characterized by the striking ‘titillation’ display, usually observed only when adult males court females. In this display, the digits of the front feet are rapidly vibrated above the eyes of the female. In our observations, both sexes performed the display, which was energetic, spontaneous, and inconclusive (in that sequences of precocious courtship typically ended when either the displayer or recipient stopped and rested, left, or started some other unrelated non-social behaviour). Displaying individuals clearly preferred conspecific recipients and often appeared to seek out specific individuals. We discuss several plausible explanations for precocious courtship in these turtles but find none entirely satisfying. The characteristics of the precocious courtship behaviour we observed most closely match those commonly listed for social play. Thus, we conclude that the most likely explanation for this behaviour is that it is a component of social play.     

A test of an antipredatory function of conspicuous plastron coloration in hatchling turtles

Bright colorations in animals are sometimes an antipredatory signal meant to startle, warn, or deter a predator from consuming a prey organism. Freshwater turtle hatchlings of many species have bright ventral coloration with high internal contrast that may have an antipredator function. We used visual modeling and field experiments to test whether the plastron coloration of Chrysemys picta hatchlings deters predators. We found that bird predators can easily distinguish hatchling turtles from their backgrounds and can easily see color contrast within the plastron. Raccoons cannot easily discriminate within-plastron color contrast but can see hatchlings against common backgrounds. Despite this, we found that brightly-colored, high contrast, replica turtles were not attacked less than low contrast replica turtles, suggesting that the bright coloration is not likely to serve an antipredatory function in this context. We discuss the apparent lack of innate avoidance of orange coloration in freshwater turtles by predators and suggest that preference and avoidance of colors are context-dependent. Since the bright colors are likely not a signal, we hypothesize that the colors may be caused by pigments deposited in tissue from maternal reserves during development. In most species, these pigments fade ontogenetically but they may have important physiological functions in species that maintain the bright coloration throughout adulthood.     

Divergent Sex-Specific Plasticity in Long-Lived Vertebrates with Contrasting Sexual Dimorphism

Sex-specific plasticity can profoundly affect sexual size dimorphism (SSD), but its influence in female-larger-SSD vertebrates remains obscure. Theory predicts that sex-specific plasticity may drive SSD evolution if the larger sex benefits from optimal-growth conditions when available (condition-dependent hypothesis), or if attaining a suboptimal size is penalized by selection (adaptive canalization hypothesis). Sex-specific plasticity enhances the size of the larger sex in male-larger-SSD turtles but whether the same occurs in female-larger species is unknown. Sexual shape dimorphism (SShD) is also widespread in nature but is understudied, and whether SShD derives from sex-specific responses to identical selective pressures or from sex-specific selection remains unclear. Here we tested whether sex-specific growth plasticity underlies the development of sexual size and shape dimorphism in the female-larger-SSD turtle, Podocnemis expansa. Individuals hatched from several incubation temperatures and were raised under common-garden conditions with varying temperature and resources. Body size and shape were plastic and sexually dimorphic, but plasticity did not differ between the sexes, opposite to the male-larger turtle Chelydra serpentina. Maternal effects (egg size) were significant on size and shape, suggesting that females increase their fitness by allocating greater energy to enhance offspring growth. Results ruled out the sex-specific plasticity hypotheses in P. expansa, indicating that SSD and SShD do not derive form differential responses to identical drivers but from sex-specific selective pressures. Our results indicate that differential plasticity does not favor males inherently, nor the larger sex, as would be expected if it was a pervasive driver of macroevolutionary patterns of sexual dimorphism across turtle lineages.     

Seasonal changes in body size,sexual size dimorphism and sex ratio in relation to mating system in an adult odonate community

Seasonal environments impose developmental time constraints on insects which can be reflected in body size and sex ratio. By tracking these two aspects in recently emerged adults of 10 species of an odonate community in a number of lakes, we investigated whether (a) body size in both sexes decreased as the flight season progressed and whether this led to seasonal changes in sexual size dimorphism (SSD); (b) SSD patterns were related to mating systems; (c) biases in sex ratio could be explained by mortality rates associated with the largest sex (e.g. in species with male-biased SSD, a female-biased sex ratio; in species with female-biased SSD, a male-biased sex ratio). Our results indicated that adults in most species, but not all, tend to reach a smaller body size as the season progressed. However, the opposite pattern was found in a few species. Predictions about the relation between SSD and mating systems were confirmed: a female-biased SSD in nonterritorial species and monomorphism for territorial species. However, predictions of biases in sex ratio according to SSD were not met in all species. Interestingly, changes in body size and SSD along the season were lake-specific in two species in which these patterns could be examined. These results, although partially supportive of environmental and sexual selection patterns acting on size and sex ratio as documented in other odonate species, indicate that we are still far from understanding seasonal constrains in these animals.     

Basking Activity is Modulated by Health State but is Constrained by Conspicuousness to Predators in Male Spanish Terrapins

Aerial basking may have several benefits for freshwater turtles in addition to thermoregulation such as removing parasites from the skin, which would improve health state. However, basking outside of water may be risky because it may expose freshwater turtles to terrestrial predators. Here, we monitored the basking activity of male Spanish terrapins (Mauremys leprosa) in a wild population of the south‐western of the Iberian Peninsula. We also measured body size, health state parameters, parasite prevalence, and limb coloration of these individuals. We aimed to examine whether basking may improve health state of turtles. The results showed that male turtles with higher basking activity were those parasitized by Hepatozoon and that had lower total white blood cell (WBC). This might indicate that turtles in worse health condition increase their time spent basking to improve their immune system. In addition, because basking might be risky, we also expected that turtles with more conspicuous coloration should reduce their basking activity to avoid being detected by potential predators. We found that infected turtles, but not uninfected ones, that spent more time basking also had less bright coloration in limb stripes. Our study provides evidence that basking activity may improve health state of terrapins, but that color conspicuity may increase costs of basking, especially for parasitized individuals. Understanding the balance between the benefits and the costs of basking might be essential for the conservation of freshwater turtle populations.     

An ethogram of body patterning behavior in the biomedically and commercially valuable squid Loligo pealei off Cape Cod, Massachusetts.

Squids have a wide repertoire of body patterns; these patterns contain visual signals assembled from a highly diverse inventory of chromatic, postural, and locomotor components. The chromatic components reflect the activity of dermal chromatophore organs that, like the postural and locomotor muscles, are controlled directly from the central nervous system. Because a thorough knowledge of body patterns is fundamental to an understanding of squid behavior, we have compiled and described an ethogram (a catalog of body patterns and associated behaviors) for Loligo pealei. Observations of this species were made over a period of three years (> or = 440 h) and under a variety of behavioral circumstances. The natural behavior of the squid was filmed on spawning grounds off Cape Cod (northwestern Atlantic), and behavioral trials in the laboratory were run in large tanks. The body pattern components--34 chromatic (including 4 polarization components), 5 postural, and 12 locomotor--are each described in detail. Eleven of the most common body patterns are also described. Four of them are chronic, or long-lasting, patterns for crypsis; an example is Banded Bottom Sitting, which produces disruptive coloration against the substrate. The remaining seven patterns are acute; they are mostly used in intraspecific communication among spawning squids. Two of these acute patterns--Lateral Display and Mate Guarding Pattern--are used during agonistic bouts and mate guarding; they are visually bright and conspicuous, which may subject the squids to predation; but we hypothesize that schooling and diurnal activity may offset the disadvantage presented by increased visibility to predators. The rapid changeability and the diversity of body patterns used for crypsis and communication are discussed in the context of the behavioral ecology of this species.     

Ethogram of Immature Green Turtles: Behavioral Strategies for Somatic Growth in Large Marine Herbivores

Animals are assumed to obtain/conserve energy effectively to maximise their fitness, which manifests itself in a variety of behavioral strategies. For marine animals, however, these behavioral strategies are generally unknown due to the lack of high-resolution monitoring techniques in marine habitats. As large marine herbivores, immature green turtles do not need to allocate energy to reproduction but are at risk of shark predation, although it is a rare occurrence. They are therefore assumed to select/use feeding and resting sites that maximise their fitness in terms of somatic growth, while avoiding predation. We investigated fine-scale behavioral patterns (feeding, resting and other behaviors), microhabitat use and time spent on each behavior for eight immature green turtles using data loggers including: depth, global positioning system, head acceleration, speed and video sensors. Immature green turtles at Iriomote Island, Japan, spent an average of 4.8 h feeding on seagrass each day, with two peaks, between 5∶00 and 9∶00, and between 17∶00 and 20∶00. This feeding pattern appeared to be restricted by gut capacity, and thus maximised energy acquisition. Meanwhile, most of the remaining time was spent resting at locations close to feeding grounds, which allowed turtles to conserve energy spent travelling and reduced the duration of periods exposed to predation. These behavioral patterns and time allocations allow immature green turtles to effectively obtain/conserve energy for growth, thus maximising their fitness.     

Female prereproductive coloration reduces mating harassment in damselflies

Conspicuous female coloration can evolve through male mate choice or via female-female competition thereby increasing female mating success. However, when mating is not beneficial, such as in pre-reproductive females, selection should favor cryptic rather than conspicuous coloration to avoid male detection and the associated harassment. Nevertheless, conspicuous female coloration occurs in many prereproductive animals, and its evolution remains an enigma. Here, I studied conspicuous female coloration in Agriocnemis femina damselflies, in which the conspicuous red color of the immature females changes to a less conspicuous green approximately a week after their emergence. I measured body size, weight, and egg numbers of the female morphs and found that red females are smaller and lighter and do not carry developed eggs. Finally, I calculated the occurrence frequency and mating frequency of red and green females in several populations over a three-year period. The results demonstrate that red females mated less frequently than green females even when red females were the abundant morph in the populations. I concluded that conspicuous female coloration is likely to function as a warning signal of sexual unprofitability, thereby reducing sexual harassment for females and unprofitable mating for males.     

不同生境间龟鳖类体型的差异

体型是动物重要的形态特征,影响动物的生境利用。为揭示龟鳖类体型与生境之间的关系,通过文献收集331种龟鳖(龟鳖目Tesudines总物种数的98.8%)的最大背甲长及其生境信息,将生境分为海洋、淡水、岛屿性陆地和大陆性陆地4种类型,再将淡水生境分为大静水、大流水、小静水、小流水和所有水域5种亚类型,大陆性陆地生境分为高地、平地和荒漠3种亚类型,从而比较不同生境类型或亚类型之间龟鳖类体型的差异。广义线性混合模型分析结果显示:1)海龟体型最大,岛屿性陆龟次之,淡水龟鳖和大陆性陆龟体型最小,且后两者差异无统计学意义。2)淡水龟鳖类的体型在5种亚类型生境间存在差异,大静水和大流水水域的体型均显著大于小静水和小流水水域,而体型在大静水与大流水水域、小静水与小流水水域之间的差异均无统计学意义,表明淡水龟鳖类体型与水域面积有关,而与水域是静水或流水无关。广布所有水域的淡水龟鳖类体型趋于中间型,且与其他4种亚类型生境中的体型之间的差异均无统计学意义。3)大陆性陆龟的体型从高地到平地再到荒漠有逐渐变大的趋势,但差异无统计学意义。本研究揭示龟鳖类的保护对策需要考虑其体型和生境面积的相关性。